Does IPSS-R down staging before transplantation improve the prognosis of patients with Myelodysplastic neoplasms?


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
10 May 2024
Historique:
accepted: 25 03 2024
received: 21 08 2023
revised: 04 03 2024
medline: 10 5 2024
pubmed: 10 5 2024
entrez: 10 5 2024
Statut: aheadofprint

Résumé

In MDS patients higher IPSS-R at transplant is associated with worse transplant outcome. Thus, it may seem beneficial to improve IPSS-R by therapeutic intervention prior to transplantation in order to "down-stage" the disease risk. However, there is no evidence to date to support this approach. A retrospective analysis of the EBMT transplant registry was performed to investigate the role of therapeutic interventions prior to transplantation with regard to changes in IPSS-R and transplant outcomes. A total of 1482 MDS patients with sufficient data to calculate IPSS-R at diagnosis and at time of transplantation were selected and analysed for transplant outcome in a multivariable Cox model including IPSS-R at diagnosis, treatment intervention, change in IPSS-R before transplant and several patient and transplant variables. Transplant outcome was unaffected by IPSS-R change in untreated patients and moderately superior in chemotherapy-treated patients with improved IPSS-R at transplant. Improved IPSS-R after hypomethylating agents (HMA) or other therapies showed no beneficial effect. However, when IPSS-R progressed after chemotherapy, (HMA) or other therapies, transplant outcome was worse than without any prior treatment. Similar results were found when reduction or increase in bone marrow (BM) blasts between diagnosis and transplantation was considered. The results show a limited benefit of IPSS-R down staging or reduction of BM blasts after chemotherapy and no benefit for HMA or other treatments and thus question the role of prior therapy in MDS patients scheduled for transplantation. The model-based survival estimates should help inform decision making for both doctors and patients.

Identifiants

pubmed: 38728380
pii: 516072
doi: 10.1182/blood.2023022273
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Society of Hematology.

Auteurs

Christof Scheid (C)

University Hospital Cologne, Cologne, Germany.

Diderik-Jan Eikema (DJ)

EBMT Leiden Study Unit, Leiden, Netherlands.

Michel Van Gelder (M)

Maastricht University Medical Center, Maastricht, Netherlands.

Urpu Salmenniemi (U)

Helsinki University Hospital, Helsinki, Finland.

Johan Maertens (J)

University Hospital Gasthuisberg, Leuven, Belgium.

Jakob R Passweg (JR)

University Hospital Basel, Basel, Switzerland.

Didier Blaise (D)

Institut Paoli Calmettes, Marseille, France.

Jennifer L Byrne (JL)

Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.

Nicolaus Kroeger (N)

University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Katja Sockel (K)

University Hospital Carl Gustav Carus, TU Dresden, German Cancer Consortium (DKTK) , Dresden, Germany, Dresden, Germany.

Patrice Chevallier (P)

Centre Hospitalo-Universitaire, Nantes, France.

Jean Henri Bourhis (JH)

Institut Gustave Roussy, Villejuif, France.

Jan J Cornelissen (JJ)

Erasmus MC, Cancer Institute, Rotterdam, Netherlands.

Henrik Sengeloev (H)

Rigshospitalet, Copenhagen, Denmark.

Jürgen Finke (J)

University Medical Center and Medical Faculty, Freiburg, Freiburg, Germany.

John A Snowden (JA)

Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.

Tobias Gedde-Dahl (T)

Department of Medicine, Oslo University Hospital, Oslo.

Jerôme Cornillon (J)

University Hospital of Saint-Etienne, Saint-Etienne, France.

Urs Schanz (U)

University Hospital of Zurich, Zurich, Switzerland.

Amit Patel (A)

in memoriam, United Kingdom.

Linda Koster (L)

EBMT Data Office, Leiden, Netherlands.

Liesbeth C de Wreede (LC)

Leiden University Medical Center, Leiden, Netherlands.

Patrick J Hayden (PJ)

School of Medicine, Trinity College Dublin, Dublin, Ireland.

Kavita Raj (K)

University College London Hospitals NHS Foundation Trust, London, United Kingdom.

Joanna Drozd-Sokolowska (J)

Central Clinical Hospital, The Medical University of Warsaw, Warsaw, Poland.

Carmelo Gurnari (C)

University of Rome Tor Vergata, Italy.

Francesco Onida (F)

Hematology and BMT Unit, ASST Fatebenefratelli-Sacco, Dept. of Oncology and Hemato-Oncology, University of Milan, Italy, Milan, Italy.

Donal P McLornan (DP)

University College Hospital, London, United Kingdom.

Marie Robin (M)

Hopital Saint Louis, Paris, France.

Ibrahim Yakoub-Agha (I)

Cellular therapy unit, Lille, France.

Classifications MeSH